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From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
Herein, we demonstrate that a bottom-up approach, based on halogen bonding (XB), can be successfully applied for the design of a new type of ionic liquid crystals (ILCs). Taking advantages of the high specificity of XB for haloperfluorocarbons and the ability of anions to act as XB-acceptors, we obt...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933245/ https://www.ncbi.nlm.nih.gov/pubmed/29630052 http://dx.doi.org/10.3791/55636 |
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author | Cavallo, Gabriella Bruce, Duncan W. Terraneo, Giancarlo Resnati, Giuseppe Metrangolo, Pierangelo |
author_facet | Cavallo, Gabriella Bruce, Duncan W. Terraneo, Giancarlo Resnati, Giuseppe Metrangolo, Pierangelo |
author_sort | Cavallo, Gabriella |
collection | PubMed |
description | Herein, we demonstrate that a bottom-up approach, based on halogen bonding (XB), can be successfully applied for the design of a new type of ionic liquid crystals (ILCs). Taking advantages of the high specificity of XB for haloperfluorocarbons and the ability of anions to act as XB-acceptors, we obtained supramolecular complexes based on 1-alkyl-3-methylimidazolium iodides and iodoperfluorocarbons, overcoming the well-known immiscibility between hydrocarbons (HCs) and perfluorocarbons (PFCs). The high directionality of the XB combined with the fluorophobic effect, allowed us to obtain enantiotropic liquid crystals where a rigid, non-aromatic, XB supramolecular anion acts as mesogenic core. X-ray structure analysis of the complex between 1-ethyl-3-methylimidazolium iodide and iodoperfluorooctane showed the presence of a layered structure, which is a manifestation of the well-known tendency to segregation of perfluoroalkyl chains. This is consistent with the observation of smectic mesophases. Moreover, all the reported complexes melt below 100 °C, and most are mesomorphic even at room temperature, despite that the starting materials were non-mesomorphic in nature. The supramolecular strategy reported here provides new design principles for mesogen design allowing a totally new class of functional materials. |
format | Online Article Text |
id | pubmed-5933245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-59332452018-05-16 From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding Cavallo, Gabriella Bruce, Duncan W. Terraneo, Giancarlo Resnati, Giuseppe Metrangolo, Pierangelo J Vis Exp Retraction Herein, we demonstrate that a bottom-up approach, based on halogen bonding (XB), can be successfully applied for the design of a new type of ionic liquid crystals (ILCs). Taking advantages of the high specificity of XB for haloperfluorocarbons and the ability of anions to act as XB-acceptors, we obtained supramolecular complexes based on 1-alkyl-3-methylimidazolium iodides and iodoperfluorocarbons, overcoming the well-known immiscibility between hydrocarbons (HCs) and perfluorocarbons (PFCs). The high directionality of the XB combined with the fluorophobic effect, allowed us to obtain enantiotropic liquid crystals where a rigid, non-aromatic, XB supramolecular anion acts as mesogenic core. X-ray structure analysis of the complex between 1-ethyl-3-methylimidazolium iodide and iodoperfluorooctane showed the presence of a layered structure, which is a manifestation of the well-known tendency to segregation of perfluoroalkyl chains. This is consistent with the observation of smectic mesophases. Moreover, all the reported complexes melt below 100 °C, and most are mesomorphic even at room temperature, despite that the starting materials were non-mesomorphic in nature. The supramolecular strategy reported here provides new design principles for mesogen design allowing a totally new class of functional materials. MyJove Corporation 2018-03-24 /pmc/articles/PMC5933245/ /pubmed/29630052 http://dx.doi.org/10.3791/55636 Text en Copyright © 2018, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Retraction Cavallo, Gabriella Bruce, Duncan W. Terraneo, Giancarlo Resnati, Giuseppe Metrangolo, Pierangelo From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding |
title | From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding |
title_full | From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding |
title_fullStr | From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding |
title_full_unstemmed | From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding |
title_short | From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding |
title_sort | from molecules to materials: engineering new ionic liquid crystals through halogen bonding |
topic | Retraction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933245/ https://www.ncbi.nlm.nih.gov/pubmed/29630052 http://dx.doi.org/10.3791/55636 |
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